PARADYM PARADYM VR 8250

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-09 for PARADYM PARADYM VR 8250 manufactured by Sorin Group Italia S.r.l. - Crm Facility.

Event Text Entries

[182554401] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[182554402] Reportedly, the patient died on (b)(6) 2020. He suffered from a ventricular fibrillation, which was correctly detected by the subject icd, but not terminated due to a shock overload. The ventricular lead impedance and coil continuity were within normal range and no noise was observed in the episodes recorded in the device memory.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1000165971-2020-00292
MDR Report Key9805709
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-09
Date of Report2020-03-09
Date of Event2020-02-01
Date Facility Aware2020-02-12
Date Mfgr Received2020-02-12
Device Manufacturer Date2010-02-05
Date Added to Maude2020-03-09
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactLAURA OUAKI
Manufacturer StreetPARC D'AFFAIRES NOVEOS 4 AVENUE R .
Manufacturer CityCLAMART 92140
Manufacturer CountryFR
Manufacturer Postal92140
Manufacturer Phone146013429
Manufacturer G1SORIN GROUP ITALIA SRL VIA CRESCENTINO 13040 SALUGGIA ITALY
Manufacturer StreetPARC D'AFFAIRES NOVEOS 4 AVENUE R .
Manufacturer CityCLAMART 92140
Manufacturer CountryFR
Manufacturer Postal Code92140
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePARADYM
Generic NameDEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Product CodeMRM
Date Received2020-03-09
Returned To Mfg2020-02-20
Model NumberPARADYM VR 8250
Catalog NumberPARADYM VR 8250
Lot Number2421
Device Expiration Date2011-02-21
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSORIN GROUP ITALIA S.R.L. - CRM FACILITY
Manufacturer AddressPARC D'AFFAIRES NOVEOS 4 AVENUE R?AUMUR . CLAMART 92140 FR 92140


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2020-03-09

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.